(Q36717856)

English

Deleted chromosome 20 from a patient with Alagille syndrome isolated in a cell hybrid through leucine transport selection: study of three candidate genes

scientific article published on November 1994

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scholarly article

1 reference

Europe PubMed Central

15 August 2017

Deleted chromosome 20 from a patient with Alagille syndrome isolated in a cell hybrid through leucine transport selection: study of three candidate genes (English)

1 reference

Europe PubMed Central

15 August 2017

Alagille syndrome

1 reference

based on heuristic

inferred from title

object named as

N Pollet

6

0 references

author name string

J F Deleuze

1

1 reference

Europe PubMed Central

15 August 2017

S Dhorne

2

1 reference

Europe PubMed Central

15 August 2017

J Hazan

3

1 reference

Europe PubMed Central

15 August 2017

E Borghi

4

1 reference

Europe PubMed Central

15 August 2017

N Raynaud

5

1 reference

Europe PubMed Central

15 August 2017

M Meunier-Rotival

7

1 reference

Europe PubMed Central

15 August 2017

J Deschatrette

8

1 reference

Europe PubMed Central

15 August 2017

D Alagille

9

1 reference

Europe PubMed Central

15 August 2017

M Hadchouel

10

1 reference

Europe PubMed Central

15 August 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 November 1994

1 reference

Europe PubMed Central

15 August 2017

number of pages

7

1 reference

based on heuristic

inferred from page(s)

Mammalian Genome

1 reference

Europe PubMed Central

15 August 2017

5

1 reference

Europe PubMed Central

15 August 2017

663-669

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Europe PubMed Central

15 August 2017

11

1 reference

Europe PubMed Central

15 August 2017

https://scigraph.springernature.com/pub.10.1007/bf00426072

0 references

Human salivary cystatin S. Cloning, sequence analysis, hybridization in situ and immunocytochemistry

1 reference

https://api.crossref.org/works/10.1007%2FBF00426072

21 January 2018

A case of a female infant with simultaneous occurrence of de novo terminal deletions on chromosome 14q and 20p.

1 reference

https://api.crossref.org/works/10.1007%2FBF00426072

21 January 2018

Murine chromosomal location of four hepatocyte-enriched transcription factors: HNf-3α, HNF-3β, HNF-3γ, and HNF-4

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pax1, a member of the paired box-containing class of developmental control genes, is mapped to human chromosome 20p11.2 by in situ hybridization (ISH and FISH)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purification, molecular cloning, and sequencing of salivary cystatin SA-1

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A molecular genetic linkage map of mouse chromosome 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of a Chinese hamster-human hybrid cell line with increased system L amino acid transport activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

46,XX/46,XX,del(20)(pter-->p12.2) mosaicism limited to fibroblasts associated with MCA/MR and severe growth deficit

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Del(20p) with manifestations of arteriohepatic dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cystatin C (CST3), the candidate gene for hereditary cystatin C amyloid angiopathy (HCCAA), and other members of the cystatin gene family are clustered on chromosome 20p11.2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alagille syndrome and deletion of 20p.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Improved techniques for the induction of mammalian cell hybridization by polyethylene glycol

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PCR primers for human chromosomes: reagents for the rapid analysis of somatic cell hybrids

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interstitial deletion of the short arm of chromosome 20 in arteriohepatic dysplasia (Alagille syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of a human genetic locus to chromosome 5 which corrects the heat sensitive lesion associated with reduced leucyl-tRNA synthetase activity in ts025Cl Chinese hamster cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Elucidation of an a and L system for amino acid transport in the human lymphoblast using a membrane filtration technique

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human cystatin C gene (CST3) is a member of the cystatin gene family which is localized on chromosome 20.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genetic linkage map of human chromosome 20 composed entirely of microsatellite markers

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Segregation analysis of Alagille syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phosphoenolpyruvate carboxykinase (GTP): characterization of the human PCK1 gene and localization distal to MODY on chromosome 20

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of short-arm of chromosome 20:46 XX, del (20) (p 11) with unusual skeletal features

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human type 2 cystatin gene family consists of eight to nine members, with at least seven genes clustered at a single locus on human chromosome 20

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A one-step efficient and specific non-radioactive non-fluorescent method for in situ hybridization of banded chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of DNA fragments from a human chromosomal subregion by Alu PCR differential hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Syndromatic hepatic ductular hypoplasia (arteriohepatic dysplasia): a clinical and hepatic histologic study of three patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Generation and fluorescent in situ hybridization mapping of yeast artificial chromosomes of 1p, 17p, 17q, and 19q from a hybrid cell line by high-density screening of an amplified library

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure and expression of the human cystatin C gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of temperature-sensitive mutants of L-cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pax 1, a member of a paired box homologous murine gene family, is expressed in segmented structures during development

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Development of intrahepatic bile ducts in humans. Possible role of laminin

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human cysteine-proteinase inhibitors: nucleotide sequence analysis of three members of the cystatin gene family

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activation pathways and human immunodeficiency virus type 1 replication are not altered in CD4+ T cells expressing the nef protein.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Arteriohepatic dysplasia (Alagille syndrome): extreme variability among affected family members

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of the human cystatin D gene (CST5) to chromosome 20p11.21 by in situ hybridization.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hepatocyte nuclear factor 3 alpha belongs to a gene family in mammals that is homologous to the Drosophila homeotic gene fork head

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of 20p 11.23----pter with normal growth hormone-releasing hormone genes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Conservation of the paired domain in metazoans and its structure in three isolated human genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal localization of seven PAX genes and cloning of a novel family member, PAX-9

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mammalian cell mutant with a temperature-sensitive leucyl-transfer RNA synthetase

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contiguous gene syndromes: a component of recognizable syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

undulated, a mutation affecting the development of the mouse skeleton, has a point mutation in the paired box of Pax 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pax: a murine multigene family of paired box-containing genes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple congenital malformations in a boy with a chromosome abnormality of the group F (46-XY, 20-P), the son of a clinically healthy subject with an analogous chromosome malformation

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening of microdeletions of chromosome 20 in patients with Alagille syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of Chinese hamster ovary cell mutants defective in the regulation of leucine transport.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7873876

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00426072

1 reference

Europe PubMed Central

15 August 2017

1 reference

Europe PubMed Central

15 August 2017

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